Boc-Tyr(Bzl)-OH

≥98%

Reagent Code: #147093
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CAS Number 54784-43-9

science Other reagents with same CAS 54784-43-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.43 g/mol
Formula C₂₁H₂₅NO₅
thermostat Physical Properties
Melting Point 110-112ºC
inventory_2 Storage & Handling
Storage 2-8ºC

description Product Description

Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions while preventing side reactions at the tyrosine hydroxyl group. The Boc group protects the alpha-amino function, while the benzyl group shields the phenolic hydroxyl, allowing stepwise assembly of complex peptides. Commonly applied in solid-phase and solution-phase synthesis of bioactive peptides, including those used in pharmaceutical research and development. Its protecting groups can be selectively removed under mild conditions, making it suitable for multi-step synthetic strategies.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,140.00
inventory 25g
10-20 days ฿4,270.00

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Boc-Tyr(Bzl)-OH
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Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions while preventing side reactions at the tyrosine hydroxyl group. The Boc group protects the alpha-amino function, while the benzyl group shields the phenolic hydroxyl, allowing stepwise assembly of complex peptides. Commonly applied in solid-phase and solution-phase synthesis of bioactive peptides, including those used in pharmaceutical research and development. Its protecting groups can be selectively re

Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions while preventing side reactions at the tyrosine hydroxyl group. The Boc group protects the alpha-amino function, while the benzyl group shields the phenolic hydroxyl, allowing stepwise assembly of complex peptides. Commonly applied in solid-phase and solution-phase synthesis of bioactive peptides, including those used in pharmaceutical research and development. Its protecting groups can be selectively removed under mild conditions, making it suitable for multi-step synthetic strategies.

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